Product NDC: | 52389-241 |
Proprietary Name: | Uricalm |
Non Proprietary Name: | Phenazopyridine Hydochloride |
Active Ingredient(s): | 99.5 mg/1 & nbsp; Phenazopyridine Hydochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52389-241 |
Labeler Name: | Alva-Amco Pharmacal Companies, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20080429 |
Package NDC: | 52389-241-12 |
Package Description: | 1 BLISTER PACK in 1 CARTON (52389-241-12) > 12 TABLET, FILM COATED in 1 BLISTER PACK (52389-241-02) |
NDC Code | 52389-241-12 |
Proprietary Name | Uricalm |
Package Description | 1 BLISTER PACK in 1 CARTON (52389-241-12) > 12 TABLET, FILM COATED in 1 BLISTER PACK (52389-241-02) |
Product NDC | 52389-241 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Phenazopyridine Hydochloride |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20080429 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Alva-Amco Pharmacal Companies, Inc. |
Substance Name | PHENAZOPYRIDINE HYDROCHLORIDE |
Strength Number | 99.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes |